Colon Cancer: Gene >> MAPK7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308406
Start	19381666:19381666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1457C>A
AA Mutation	p.Ser486Tyr(p.S486Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308406
Start	19380751:19380751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773156619
CDS Mutation	c.542G>A
AA Mutation	p.Arg181His(p.R181H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308406
Start	19379932:19379932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383G>A
AA Mutation	p.Gly128Asp(p.G128D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308406
Start	19381170:19381170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.961C>A
AA Mutation	p.Leu321Ile(p.L321I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308406
Start	19380796:19380796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.587T>C
AA Mutation	p.Leu196Pro(p.L196P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308406
Start	19382260:19382260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144078337
CDS Mutation	c.1957G>A
AA Mutation	p.Ala653Thr(p.A653T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308406
Start	19382432:19382432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2129T>C
AA Mutation	p.Val710Ala(p.V710A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308406
Start	19381157:19381157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376826566
CDS Mutation	c.948C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308406
Start	19379050:19379050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308406
Start	19380890:19380890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.681C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MAPK7

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308406
Start	19379819:19379819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.270C>T
Mutation Classification	Silent
Feature Type	Transcript